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一例罕见的肛周颗粒细胞瘤:病例报告及文献复习

A rare case of perianal granular cell tumor: case report and literature review.

作者信息

Kelly Emily F, Stein Alan A, Ma Xiaoling Charlene, Yeguez Jose

机构信息

Department of Surgery, Boca Raton Regional Hospital, Charles E. Schmidt College of Medicine, Florida Atlantic University, Boca Raton, FL, USA.

出版信息

J Surg Case Rep. 2017 Jun 6;2017(6):rjw186. doi: 10.1093/jscr/rjw186. eCollection 2017 Jun.

DOI:10.1093/jscr/rjw186
PMID:28603602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5460004/
Abstract

Granular cell tumor (GCT) is a rare submucosal neoplasm most commonly localized in the oral mucosa; with one-third of all cases found in the tongue, with less than 30 cases of perianal GCT reported in the literature, making it a rare anal neoplasm. Wide local excision is the gold standard of treatment and follow-up includes annual colonoscopy due to the high incidence of reoccurrence. Here we describe a rare case of benign perianal GCT in a 29-year-old female who presented asymptomatically; however, pathology report revealed a S100 positive immunostaining pattern. GCT is an important differential to be included when evaluating a patient with an asymptomatic perianal submucosal lesion. Since GCT and Squamous Cell Carcinoma present with similar pseudoepitheliomatous hyperplasia of the epithelium it is important that a biopsy and immunohistochemical analysis be performed to allow for accurate diagnosis and appropriate treatment.

摘要

颗粒细胞瘤(GCT)是一种罕见的黏膜下肿瘤,最常见于口腔黏膜;所有病例中有三分之一发生在舌部,文献报道的肛周GCT病例少于30例,使其成为一种罕见的肛门肿瘤。广泛局部切除是治疗的金标准,由于复发率高,随访包括每年进行结肠镜检查。在此,我们描述了一例29岁无症状女性的罕见良性肛周GCT病例;然而,病理报告显示免疫染色模式为S100阳性。在评估无症状肛周黏膜下病变的患者时,GCT是一个需要鉴别的重要疾病。由于GCT和鳞状细胞癌表现出类似的上皮假上皮瘤样增生,因此进行活检和免疫组化分析以实现准确诊断和适当治疗非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be26/5460004/69bfcba23363/rjw186f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be26/5460004/69bfcba23363/rjw186f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be26/5460004/69bfcba23363/rjw186f01.jpg

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本文引用的文献

1
A rare case of granular cell tumor of the anal region: diagnostic difficulty to masses in the anal area.一例罕见的肛管颗粒细胞瘤:肛管区肿物的诊断难点
Int Surg. 2014 Jan-Feb;99(1):45-7. doi: 10.9738/INTSURG-D-13-00149.1.
2
Recurrent granular cell tumor of the anal-perianal region: how much anal sphincter can be resected?肛门-肛周区域复发性颗粒细胞瘤:可切除多少肛门括约肌?
Tech Coloproctol. 2014 Jun;18(6):597-600. doi: 10.1007/s10151-013-1043-6. Epub 2013 Jul 16.
3
Malignant granular cell tumor of the anal-perianal region and suprarenal hyperplasia: a casual association?
肛门-肛周区域恶性颗粒细胞瘤与肾上腺增生:一种偶然关联?
Indian J Dermatol. 2010 Oct;55(4):403-5. doi: 10.4103/0019-5154.74573.
4
Anal region: an unusual location of granular cell tumour.
Int J Colorectal Dis. 2011 Jun;26(6):811-2. doi: 10.1007/s00384-010-1061-z. Epub 2010 Oct 1.
5
Perianal granular cell tumor: report of a case and review of the literature.肛周颗粒细胞瘤:1例报告并文献复习
Tumori. 2009 Jul-Aug;95(4):538-41. doi: 10.1177/030089160909500424.
6
Granular cell tumor of colon: report of a case and review of literature.结肠颗粒细胞瘤:1例报告并文献复习
World J Gastroenterol. 2004 Aug 15;10(16):2452-4. doi: 10.3748/wjg.v10.i16.2452.
7
[Benign granular cell anal tumor].[良性颗粒细胞肛门肿瘤]
Presse Med. 2003 Feb 8;32(5):221-2.
8
Granular cell tumor--a unique neoplasm of the internal anal sphincter: report of a case.颗粒细胞瘤——一种独特的肛门内括约肌肿瘤:病例报告
Dis Colon Rectum. 2000 Oct;43(10):1444-6; discussion 1447. doi: 10.1007/BF02236643.
9
Granular-cell tumors (myoblastomas) of the anal region.
Dis Colon Rectum. 1978 Sep;21(6):413-7. doi: 10.1007/BF02586717.